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FDA 510(k)

PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR

K-Number: K893199 · 1989-06-16

ApplicantAllergan Medical Optics
Decision Date1989-06-16
Product CodeHNR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR is the device name listed in this FDA 510(k) record. The listed applicant is Allergan Medical Optics. It received FDA 510(k) clearance on 1989-06-16 under 510(k) number K893199. The device is classified under product code HNR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR?

PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR is a medical device that received FDA 510(k) clearance on 1989-06-16. The listed applicant is Allergan Medical Optics. The 510(k) number is K893199.

When did PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR receive FDA 510(k) clearance?

PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR received FDA 510(k) clearance on 1989-06-16, under 510(k) number K893199.

Who is the listed applicant for PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR?

The FDA 510(k) record lists Allergan Medical Optics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR?

The FDA product code for PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR is HNR.

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Other records listing Allergan Medical Optics as applicant

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Related Devices (Code: HNR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K022835STEPHENS DISPOSABLE FORCEPSStephens InstrumentsK895434ALCON FOLDING FORCEPSAlcon LaboratoriesK891487SOFT LENS FOLDING BLOCKWestern Medical Products, Inc.K885230MCDONALD FOLDING FORCEPSAlcon LaboratoriesK881049BRADBURY INTRAOCULAR RETINAL KIT CAT #200Microline Pentax, Inc.K883197IOL IMPLANTATION FORCEPSD & D Surgical

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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